Guest guest Posted June 21, 2006 Report Share Posted June 21, 2006 Do you sand by hand or use a power sander? lol. If anyone who did not understand our symptoms and issues read these posts they'd think we'd all gone " whoo-hoo " . Sanding sounds good if your hands are up to it. I have to ask you what grit you use though. I think you are probably right about the lotions on the market. We have become microwave society. We want it all NOW so we tend to take a " feel good " approach and the manufacturers know this about us. They've studied us and they did not need alien probes to do it. So they make skin " care " products that give us instant results rather than long term therapy....and we buy them. I've got to go read some labels now and then I'm off to visit the skin care aisle of Home Depot to pick up a Black and Decker exfoliator. Wonder if WD-40 would work on our joints? -Betz Betsy Jack itsbetsy@... [ ] Re: Weird Question #1105 i use sandpaper on my callouses (same concept as a file on nails). works like a charm. in regards to mosturizers. .. i believe about 95% of all commercially available mosturizers (ie available at a drug store etc) contain alcohols. these feel soft and silky going on and for several hours, but have a net effect of actually drying out the skin more than moisturizing them. so they actaully make things worse. i think i heard there are very few that actually are good to use.(i dont use them) but i seem to recall vasoline was on the good list. just my 2 cents, cfsguy > > I have been worried about my post suggesting that people shave their feet. I later thought about it and I don't think it will be such a bright idea for everyone... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 21, 2006 Report Share Posted June 21, 2006 I, too, get the " horny feet " , along with cracking and scaling on the heels. Both are vastly improved since starting Remicade. Before the treatment, I'd use a pumice stone on them, and my pedicurist used a razor thingie to reduce their thickness. Also, I once had psorasis and peeling so bad on both my hands that I developed secondary infections on both palms. That was soooo attractive, let me tell ya. Especially since I was new in town, trying to make friends, and trying to impress a new boss and coworkers. - ===================================================== Stein EBAY: http://search.ebay.com/_W0QQfgtpZ1QQfrppZ25QQsassZalliQ5fatticQ5f42 WEBSITE: http://www.noblefusion.com/astein BLOG: http://www.livejournal.com/users/astein142/ ----------------------------------------------------- __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 22, 2006 Report Share Posted June 22, 2006 Get out. -Betz Betsy Jack itsbetsy@... [Editor's Note: It's true. lives in Kansas and his neighbor is the Tin Man. I'm about to break out into " Follow the Yellow Brick Road " from " The Wiz " . Kathy F.} [ ] Re: Weird Question #1105 Funny you should ask... I have a neighbor who swears by it... michael > .. Wonder if WD-40 would work on our joints? -Betz > > Betsy Jack itsbetsy@... > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 23, 2006 Report Share Posted June 23, 2006 Wonder if WD-40 would work on our joints? -Betz Hi all, Interesting question...my grandfather (from whom I inherited the PA gift) swore by WD-40 and would spray it on his joints. Course, he also slathered mustard on everything he ate claiming that it was the " indians " cure for cancer...the indians cured cancer and didn't share it with us...who knew warm blessings, jane __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 23, 2006 Report Share Posted June 23, 2006 I have a question for everyone. Has anyone had their elbow lock up with Psoriatic Arthritis? My shoulders and hip have pain on both sides and feel hot to the touch. Do you have this too. I was told to drink plenty of water with my meds. When I don't drink as much some days, I get real flushed and hot. I'm thinking my blood pressure is up too. However, since I've put the connection of the two together, I make sure I drink my WATER!!! I am concerned about my blood pressure though. My bottom number is always in the upper 80's. So do you think my hot flashes, sweating comes from lacking of drink enough water or BP? It does seem less bothersome the days I concentrate on drinking WATER. Has anyone elso experienced this? Rhonda X > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 23, 2006 Report Share Posted June 23, 2006 Kathy...you've been cracking me up lately? What medication did you say you are on? And I was the BAD witch in The Wiz...but I don' t have nearly as many credits as Hollywood Jenn...or what was it you called her? And now " I Feel Pretty " is stuck in my head. I have 2 work days left with my soon to be old boss...might as well torment him with that song before I go. Heh Heh Heh. Interviewing for a job in car sales next week. Did that when I was 21...over half my life ago. Back when you had to crank the cars. But this could work for me. If you need a car....wait. And then maybe you can come to Rhinebeck and get a sweet deal on a Jeep. -Betz (Editor's Note - could it be that I have 11 working days left before retirement? I'll certainly buy a jeep from you but as a retiree, I'll have no money. Sorry about planting that earworm (ie song you can't get out of your head) but be glad I didn't sing " Edelweiss, edelweiss... " . Oops, I did it again. Kathy F. ) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 24, 2006 Report Share Posted June 24, 2006 Hi, I get the same symptoms as you and its cause by PA but the heat and sweating when I had it the methotrexate can cause it which my doctor told me and it all be like hot flashes but different cause you don't sweet like hot flashes. Drink a lot of water is good cause of the meds we take and we can easily be dehydrated. take care Re: [ ] Re: Weird Question #1105 I have a question for everyone. Has anyone had their elbow lock up with Psoriatic Arthritis? My shoulders and hip have pain on both sides and feel hot to the touch. Do you have this too. I was told to drink plenty of water with my meds. When I don't drink as much some days, I get real flushed and hot. I'm thinking my blood pressure is up too. However, since I've put the connection of the two together, I make sure I drink my WATER!!! I am concerned about my blood pressure though. My bottom number is always in the upper 80's. So do you think my hot flashes, sweating comes from lacking of drink enough water or BP? It does seem less bothersome the days I concentrate on drinking WATER. Has anyone elso experienced this? Rhonda X > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 25, 2006 Report Share Posted June 25, 2006 In a message dated 6/24/2006 5:14:34 A.M. Pacific Daylight Time, michaelr_321@... writes: I kid you not... He has applied it to his hands every day since he was diagnosed with arthritis in them 39 years ago. I can't say it worked over medication or what, but his hands have been arthritis free over the rest of him... Go figure... (and actually his name is Ed) ...sounds like the Dad from My Big Fat Greek Wedding who was always spraying everyone with Windex... Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 25, 2006 Report Share Posted June 25, 2006 In a message dated 6/24/2006 5:28:32 A.M. Pacific Daylight Time, itsbetsy@... writes: could it be that I have 11 working days left before retirement? Kathy...I wish there was some way we could have a retirement party for you on this board:-) You sound so happy, even happier than normal, so you must be looking forward to it...I for one though am very happy that you aren't retiring from our board:-) [Editor's Note: , you are so sweet. I wish we could have a party - but to celebrate our support for one another. Yes, I am thrilled that I am retiring. I had a very rough winter physically and last November when my boss died suddenly from an infection, I said to myself that I wanted to enjoy some of my life before being confined to a wheelchair, if in fact that's where I'm headed. I'd also probably be a pretty happy person if confined to a chair, but it is just so much easier to get around if you're not. So, I decided to quit when I turn 57 which is next month. I still love what I do, but the sheer stress of living and working in NYC can take a toll, especially when dealing with the disease for 41 years. I am very much looking forward to being able to rest on the days when I need to, to fighting the disease with more physical therapy and to doing volunteer work that I no longer had the energy to do. I think the best of my life is just starting, regardless of what the disease has in store for me. Thanks for the really nice thoughts! Best, Kathy F.] Quote Link to comment Share on other sites More sharing options...
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